Canonical Allele Identifier: CA1041738265

Gene: CRYGD

Linked Data

• dbSNP Id: rs1694924480

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208124050_208124051del , CM000664.2:g.208124050_208124051del	GRCh38
NC_000002.11:g.208988774_208988775del , CM000664.1:g.208988774_208988775del	GRCh37
NC_000002.10:g.208697019_208697020del	NCBI36
NG_008039.1:g.5541_5542del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264376.5:c.252+63_252+64del MANE Select	ENSP00000264376.4:n.252+63_252+64del
ENST00000264376.4:c.252+63_252+64del	ENSP00000264376.4:n.252+63_252+64del
NM_006891.3:c.252+63_252+64del	NP_008822.2:n.252+63_252+64del
NR_038437.1:n.97+4825_97+4826del
NM_006891.4:c.252+63_252+64del MANE Select	NP_008822.2:n.252+63_252+64del